Haynes Lab:Notebook/Short Projects/2015/03/09

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PCR-verify activation domain primers
Try different cDNA libraries for the CARM1 and MYB fragment to account for any mutations or deletions

  1. U2OS C002, 1:1000 cDNA dilution; CARM1 = 1827 bp: CARM1 F1/ CARM1 R1; MYB = 159 bp: MYB F1/ MYB R1.
  2. SKNSH C001, 1:1000 cDNA dilution; same.
  3. K562 C001, 1:1000 cDNA dilution; same.


Reagent Rxn1 Rxn2 Rxn3 Expected:
1. U2OS CARM1 = 1827 bp
7. U2OS MYB = 159 bp
2. SKNSH CARM1 = 1827 bp
8. SKNSH MYB = 159 bp
3. K562 CARM1 = 1827 bp
9. K562 MYB = 159 bp
Hover name
10 μL/lane, 1% agarose; Ladder
Template 1.0 1.0 1.0
10 uM fwd primer 1.0 1.0 1.0
10 uM rev primer 1.0 1.0 1.0
2x GoTaq green 12.5 12.5 12.5
dH2O 9.5 9.5 9.5
  25.0 25.0 25.0

Program: GOTAQ35cyc

  • 95°C, 3 min
  • 35x[95°C, 30 sec; 57°C, 30 sec; 72°C, 2 min]
  • 72°C, 5 min
  • 4°C ∞


  • Cycle times adjusted for Gotaq protocol; the camera is damaged, so manual imaging techniques are necessary.





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